Glucocorticoid-induced tumour necrosis factor receptor expression: a potential molecular link between steroid intake and complicated diverticulitis?

Colorectal Dis. 2012 Oct;14(10):1276-86. doi: 10.1111/j.1463-1318.2012.02967.x.

Abstract

Aim: Immunosuppression and steroid medication have been identified as risk factors for complicated sigmoid diverticulitis. The underlying molecular mechanisms have not yet been elucidated. We hypothesized that glucocorticoid-induced tumour necrosis factor receptor (GITR) and matrix metalloproteinase-9 (MMP-9) might play a role.

Method: GITR and MMP-9 were analysed at protein [immunohistochemistry/immunofluorescence (IF)] and messenger RNA level (real-time polymerase chain reaction) in surgical specimens with complicated and non-complicated diverticulitis (n=101). IF double staining and regression analysis were performed for both markers. GITR expression was correlated with clinical data and its usefulness as a diagnostic test was investigated.

Results: High GITR expression (≥41%) was observed in the inflammatory infiltrate in complicated diverticulitis, in contrast to non-complicated diverticulitis where GITR expression was low (P<0.001). High GITR expression was significantly associated with steroid use and pulmonary diseases (both P<0.001). MMP-9 expression correlated with GITR expression (R(2) =0.7268, P<0.0001, r=0.85) as demonstrated with IF double-staining experiments. Co-labelling of GITR with CD68, but not CD15, suggested that GITR-expressing cells in diverticulitis are macrophages. GITR expression was superior to C-reactive protein (CRP), white cell count and temperature in distinguishing complicated and non-complicated diverticulitis.

Conclusions: Our results suggest that GITR expression in inflammatory cells might potentially indicate a molecular link between steroid use and complicated forms of acute sigmoid diverticulitis. Increased MMP-9 expression by GITR signalling might explain the morphological changes in the colonic wall of perforated and phlegmonous diverticulitis. Analysis of soluble GITR might be a promising strategy for future research.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Antigens, CD / metabolism
  • Antigens, Differentiation, Myelomonocytic / metabolism
  • Biomarkers / metabolism
  • Case-Control Studies
  • Diverticulitis, Colonic / chemically induced
  • Diverticulitis, Colonic / complications
  • Diverticulitis, Colonic / diagnosis
  • Diverticulitis, Colonic / metabolism*
  • Female
  • Fucosyltransferases / metabolism
  • Glucocorticoid-Induced TNFR-Related Protein / metabolism*
  • Humans
  • Immunohistochemistry
  • Immunosuppressive Agents / adverse effects*
  • Lewis X Antigen / metabolism
  • Macrophages / metabolism
  • Male
  • Matrix Metalloproteinase 9 / metabolism*
  • Middle Aged
  • Odds Ratio
  • Prospective Studies
  • ROC Curve
  • Real-Time Polymerase Chain Reaction
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sigmoid Diseases / chemically induced
  • Sigmoid Diseases / complications
  • Sigmoid Diseases / diagnosis
  • Sigmoid Diseases / metabolism*
  • Steroids / adverse effects*

Substances

  • Antigens, CD
  • Antigens, Differentiation, Myelomonocytic
  • Biomarkers
  • CD68 antigen, human
  • Glucocorticoid-Induced TNFR-Related Protein
  • Immunosuppressive Agents
  • Lewis X Antigen
  • Steroids
  • TNFRSF18 protein, human
  • FUT4 protein, human
  • Fucosyltransferases
  • Matrix Metalloproteinase 9